BIOMARKERS

Molecular Biopsy of Human Tumors

- a resource for Precision Medicine *

241 related articles for article (PubMed ID: 31980437)

  • 1. Six1 proteins with human branchio-oto-renal mutations differentially affect cranial gene expression and otic development.
    Shah AM; Krohn P; Baxi AB; Tavares ALP; Sullivan CH; Chillakuru YR; Majumdar HD; Neilson KM; Moody SA
    Dis Model Mech; 2020 Mar; 13(3):. PubMed ID: 31980437
    [TBL] [Abstract][Full Text] [Related]  

  • 2. Sobp modulates the transcriptional activation of Six1 target genes and is required during craniofacial development.
    Tavares ALP; Jourdeuil K; Neilson KM; Majumdar HD; Moody SA
    Development; 2021 Sep; 148(17):. PubMed ID: 34414417
    [TBL] [Abstract][Full Text] [Related]  

  • 3. Mcrs1 interacts with Six1 to influence early craniofacial and otic development.
    Neilson KM; Keer S; Bousquet N; Macrorie O; Majumdar HD; Kenyon KL; Alfandari D; Moody SA
    Dev Biol; 2020 Nov; 467(1-2):39-50. PubMed ID: 32891623
    [TBL] [Abstract][Full Text] [Related]  

  • 4. EYA1 mutations associated with the branchio-oto-renal syndrome result in defective otic development in Xenopus laevis.
    Li Y; Manaligod JM; Weeks DL
    Biol Cell; 2010 Feb; 102(5):277-92. PubMed ID: 19951260
    [TBL] [Abstract][Full Text] [Related]  

  • 5. Mutations in SIX1 Associated with Branchio-oto-Renal Syndrome (BOR) Differentially Affect Otic Expression of Putative Target Genes.
    Mehdizadeh T; Majumdar HD; Ahsan S; Tavares ALP; Moody SA
    J Dev Biol; 2021 Jun; 9(3):. PubMed ID: 34208995
    [TBL] [Abstract][Full Text] [Related]  

  • 6. Pa2G4 is a novel Six1 co-factor that is required for neural crest and otic development.
    Neilson KM; Abbruzzesse G; Kenyon K; Bartolo V; Krohn P; Alfandari D; Moody SA
    Dev Biol; 2017 Jan; 421(2):171-182. PubMed ID: 27940157
    [TBL] [Abstract][Full Text] [Related]  

  • 7. SIX1 mutations cause branchio-oto-renal syndrome by disruption of EYA1-SIX1-DNA complexes.
    Ruf RG; Xu PX; Silvius D; Otto EA; Beekmann F; Muerb UT; Kumar S; Neuhaus TJ; Kemper MJ; Raymond RM; Brophy PD; Berkman J; Gattas M; Hyland V; Ruf EM; Schwartz C; Chang EH; Smith RJ; Stratakis CA; Weil D; Petit C; Hildebrandt F
    Proc Natl Acad Sci U S A; 2004 May; 101(21):8090-5. PubMed ID: 15141091
    [TBL] [Abstract][Full Text] [Related]  

  • 8. Mcrs1 is required for branchial arch and cranial cartilage development.
    Keer S; Cousin H; Jourdeuil K; Neilson KM; Tavares ALP; Alfandari D; Moody SA
    Dev Biol; 2022 Sep; 489():62-75. PubMed ID: 35697116
    [TBL] [Abstract][Full Text] [Related]  

  • 9. Genetic research progress in branchio
    Chen A; Ling J; Feng Y
    Zhong Nan Da Xue Xue Bao Yi Xue Ban; 2022 Jan; 47(1):129-138. PubMed ID: 35545373
    [TBL] [Abstract][Full Text] [Related]  

  • 10. Microarray identification of novel genes downstream of Six1, a critical factor in cranial placode, somite, and kidney development.
    Yan B; Neilson KM; Ranganathan R; Maynard T; Streit A; Moody SA
    Dev Dyn; 2015 Feb; 244(2):181-210. PubMed ID: 25403746
    [TBL] [Abstract][Full Text] [Related]  

  • 11. Generation of a new six1-null line in Xenopus tropicalis for study of development and congenital disease.
    Coppenrath K; Tavares ALP; Shaidani NI; Wlizla M; Moody SA; Horb M
    Genesis; 2021 Dec; 59(12):e23453. PubMed ID: 34664392
    [TBL] [Abstract][Full Text] [Related]  

  • 12. Biochemical and functional characterization of six SIX1 Branchio-oto-renal syndrome mutations.
    Patrick AN; Schiemann BJ; Yang K; Zhao R; Ford HL
    J Biol Chem; 2009 Jul; 284(31):20781-90. PubMed ID: 19497856
    [TBL] [Abstract][Full Text] [Related]  

  • 13. SIX1 mutation screening in 247 branchio-oto-renal syndrome families: a recurrent missense mutation associated with BOR.
    Kochhar A; Orten DJ; Sorensen JL; Fischer SM; Cremers CW; Kimberling WJ; Smith RJ
    Hum Mutat; 2008 Apr; 29(4):565. PubMed ID: 18330911
    [TBL] [Abstract][Full Text] [Related]  

  • 14. Eya1 regulates the growth of otic epithelium and interacts with Pax2 during the development of all sensory areas in the inner ear.
    Zou D; Silvius D; Rodrigo-Blomqvist S; Enerbäck S; Xu PX
    Dev Biol; 2006 Oct; 298(2):430-41. PubMed ID: 16916509
    [TBL] [Abstract][Full Text] [Related]  

  • 15. Mutational analysis of EYA1, SIX1 and SIX5 genes and strategies for management of hearing loss in patients with BOR/BO syndrome.
    Song MH; Kwon TJ; Kim HR; Jeon JH; Baek JI; Lee WS; Kim UK; Choi JY
    PLoS One; 2013; 8(6):e67236. PubMed ID: 23840632
    [TBL] [Abstract][Full Text] [Related]  

  • 16. Six1 and Irx1 have reciprocal interactions during cranial placode and otic vesicle formation.
    Sullivan CH; Majumdar HD; Neilson KM; Moody SA
    Dev Biol; 2019 Feb; 446(1):68-79. PubMed ID: 30529252
    [TBL] [Abstract][Full Text] [Related]  

  • 17. Branchio-oto-renal syndrome: detection of EYA1 and SIX1 mutations in five out of six Danish families by combining linkage, MLPA and sequencing analyses.
    Sanggaard KM; Rendtorff ND; Kjaer KW; Eiberg H; Johnsen T; Gimsing S; Dyrmose J; Nielsen KO; Lage K; Tranebjaerg L
    Eur J Hum Genet; 2007 Nov; 15(11):1121-31. PubMed ID: 17637804
    [TBL] [Abstract][Full Text] [Related]  

  • 18. Using Xenopus to discover new candidate genes involved in BOR and other congenital hearing loss syndromes.
    Neal SJ; Rajasekaran A; Jusić N; Taylor L; Read M; Alfandari D; Pignoni F; Moody SA
    J Exp Zool B Mol Dev Evol; 2024 May; 342(3):212-240. PubMed ID: 37830236
    [TBL] [Abstract][Full Text] [Related]  

  • 19. Phenotypic and molecular basis of SIX1 variants linked to non-syndromic deafness and atypical branchio-otic syndrome in South Korea.
    Lee S; Yun Y; Cha JH; Han JH; Lee DH; Song JJ; Park MK; Lee JH; Oh SH; Choi BY; Lee SY
    Sci Rep; 2023 Jul; 13(1):11776. PubMed ID: 37479820
    [TBL] [Abstract][Full Text] [Related]  

  • 20. Mutation screening of the EYA1, SIX1, and SIX5 genes in a large cohort of patients harboring branchio-oto-renal syndrome calls into question the pathogenic role of SIX5 mutations.
    Krug P; Morinière V; Marlin S; Koubi V; Gabriel HD; Colin E; Bonneau D; Salomon R; Antignac C; Heidet L
    Hum Mutat; 2011 Feb; 32(2):183-90. PubMed ID: 21280147
    [TBL] [Abstract][Full Text] [Related]  

    [Next]    [New Search]
    of 13.